Cool paper #1: duplex-sequencing to detect ultra-rare variants
TwinStrand Duplex Sequencing Technology
GitHub - Kennedy-Lab-UW/Duplex-Sequencing
Duplex Proximity Sequencing (Pro-Seq): A method to improve DNA sequencing accuracy without the cost of molecular barcoding redundancy | PLOS ONE
TwinStrand's Duplex Sequencing Goes Deep: When it comes to detection of low frequency variants, Jesse Salk's technology is one in (ten) million: GEN Edge: Vol 2, No 1
What are UMIs and why are they used in high-throughput sequencing? | DNA Technologies Core
SinoDuplex: An Improved Duplex Sequencing Approach to Detect Low-frequency Variants in Plasma cfDNA Samples | Semantic Scholar
Duplex sequencing - Wikiwand
Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI | Scientific Reports
Design of single-end duplex-UMI adapter. (a) Schematics showing how... | Download Scientific Diagram
Duplex sequencing - Wikipedia
Detecting ultralow-frequency mutations by Duplex Sequencing. - Abstract - Europe PMC
Estimating somatic mutation rates by Duplex Sequencing in non-model organisms: Daphnia magna as a case study | bioRxiv
Duplex Sequencing
Katherine Lawrence: Advances in duplex basecalling - YouTube
Research Sequencing Service: Supported Analysis Pipelines | Research | Dept. of Laboratory Medicine & Pathology | UW Medicine
Inigo Martincorena on Twitter: "Over 4 years of iterative refinement, Rob Osborne and @AbascalFed identified sources of error in duplex sequencing: end repair, nick extension, mapping errors, DNA contamination… devising solutions to
Detecting Rare Mutations and DNA Damage with Sequencing-Based Methods: Trends in Biotechnology
Family reunion via error correction: an efficient analysis of duplex sequencing data | BMC Bioinformatics | Full Text
TwinStrand Duplex Sequencing Technology
File:Duplex sequencing overview.svg - Wikimedia Commons
Single-molecule, quantitative detection of low-abundance somatic mutations by high-throughput sequencing | Science Advances
Cool paper #1: duplex-sequencing to detect ultra-rare variants
Oxford Nanopore Tech Update: new Duplex method for Q30 nanopore single molecule reads, PromethION 2, and more
Streamlined analysis of duplex sequencing data with Du Novo | Genome Biology | Full Text
